Document Detail


Alteration of xanthine oxidase activity in sinusoidal endothelial cells and morphological changes of Kupffer cells in hypoxic and reoxygenated rat liver.
MedLine Citation:
PMID:  7768504     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In the model of the perfused rat liver, we investigated the alterations of sinusoidal cells in the pathogenesis of liver injury caused by hypoxia and reperfusion. In sinusoidal endothelial cells, the activity of xanthine oxidase (XOX), a cytoplasmic marker enzyme, was located cytochemically and determined biochemically. Kupffer cells, identified by their endogenous peroxidase staining, were studied with regard to changes in their ultrastructure. In our experiments, parenchymal cells were shown to be severely damaged in contrast to sinusoidal lining cells, which showed minor signs of injury. In comparison with the control group, XOX activity increased significantly in the sinusoidal endothelial cells after low-flow hypoxia; however, after reoxygenation of only 5 minutes, that activity was lower after hypoxia but higher after control perfusion. In Kupffer cells, hypoxia resulted in a strong suppression of phagocytic and endocytotic activity and in a disappearance of the lamellopodia. Kupffer cells were flattened, resembling sinusoidal endothelial cells. After reoxygenation phagocytic vesicles, lamellopodia, and cell volume of Kupffer cells increased markedly in comparison with the control group. In the hypoxia/reperfusion injury model, our observations revealed significant alterations of sinusoidal lining cells. It appears that sinusoidal endothelial cells respond to the hypoxic phase by producing oxygen-derived free radicals and that Kupffer cells respond to the subsequent reperfusion phase by activation followed by the release of toxic mediators.
Authors:
S Angermüller; M Schunk; K Kusterer
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Hepatology (Baltimore, Md.)     Volume:  21     ISSN:  0270-9139     ISO Abbreviation:  Hepatology     Publication Date:  1995 Jun 
Date Detail:
Created Date:  1995-06-30     Completed Date:  1995-06-30     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  8302946     Medline TA:  Hepatology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1594-601     Citation Subset:  IM    
Affiliation:
Department of Anatomy and Cell Biology II, University of Heidelberg, Germany.
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MeSH Terms
Descriptor/Qualifier:
Animals
Anoxia
Cell Nucleus / ultrastructure
Endothelium / enzymology,  ultrastructure
Female
Glutamate Dehydrogenase / analysis
Kupffer Cells / cytology*,  pathology
L-Lactate Dehydrogenase / analysis
Liver / enzymology,  physiology*,  physiopathology
Microbodies / ultrastructure
Oxygen / pharmacology
Rats
Rats, Wistar
Reperfusion
Reperfusion Injury / enzymology,  physiopathology
Xanthine Oxidase / metabolism*
Chemical
Reg. No./Substance:
7782-44-7/Oxygen; EC 1.1.1.27/L-Lactate Dehydrogenase; EC 1.17.3.2/Xanthine Oxidase; EC 1.4.1.2/Glutamate Dehydrogenase

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